scholarly journals Prostatic utricle cyst causing ejaculatory duct obstruction and persistent haemtospermia

2021 ◽  
Author(s):  
Ali Alsmair
2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Shulin Guo ◽  
Donghua Xie ◽  
Xiangfei He ◽  
Chuance Du ◽  
Lunfeng Zhu ◽  
...  

To describe a novel technique of transurethral seminal vesiculoscopy using a pediatric ureteroscope in the diagnosis and management of persistent hematospermia, a retrospective study was carried out for 20 patients with recurrent hematospermia whom we evaluated and treated using a 6–7.5F (6F front end and 7.5F rear end) pediatric ureteroscope from August 2009 to September 2013. For the 20 patients, the age ranges from 25 to 48 years with a mean age of 36 years. The duration of the hematospermia ranges from 6 to 48 months with a mean duration of 18 months. Transurethral seminal vesiculoscopy was successfully performed in the 20 cases and the mean operative time was 35 min (ranges from 25 to 90 min). Among the 20 patients, 11 patients were found to have seminal vesiculitis, five were with seminal vesicle stone, one was with prostatic utricle stone, one was with prostate cyst, and one was with ejaculatory duct obstruction. The mean follow-up period was 7 months (ranged from 6 to 12 months). Hematospermia in 19 cases disappeared after the surgery and only in one patient the hematospermia recurred 6 months after the surgery. The cure rate was 95%. This study indicated that transurethral seminal vesiculoscopy could be performed easily using a semirigid pediatric ureteroscope with few complications and is an effective therapeutic approach for persistent hematospermia.


2021 ◽  
Vol 14 (1) ◽  
pp. e239254
Author(s):  
Harkirat Singh Talwar ◽  
Ankur Mittal ◽  
Tushar Aditya Narain ◽  
Vikas Kumar Panwar

Congenital malformations of the seminal vesicles (SVs) are rare and are associated with abnormalities of the ipsilateral urinary tracts as embryologically both the ureteral buds and SVs arise from the mesonephric ducts. The triad of SV cysts, ipsilateral renal agenesis and ejaculatory duct obstruction is known as the Zinner syndrome. We, herein, present three very rare presentations of Zinner syndrome. Case 1 presented with haematuria, and was found to have a large SV cyst with stones and underwent a robotic cyst excision. Case 2 presented with primary infertility, and was found to have a variant of Zinner syndrome. Case 3 was a known case of chronic kidney disease on maintenance haemodialysis who presented with fever and oliguria. He was found to have Zinner syndrome and underwent aspiration of SV abscess. To the best of our knowledge, such varying presentations of Zinner syndrome have been rarely reported thus far.


2001 ◽  
Vol 39 (1) ◽  
pp. 24-29 ◽  
Author(s):  
Yaşar Özgök ◽  
Yaşar Özgök ◽  
Özgür Tan ◽  
Özgür Tan ◽  
Mete Kilciler ◽  
...  

2013 ◽  
Vol 21 (2) ◽  
pp. 293-302
Author(s):  
Xiang-An Tu ◽  
Jin-Tao Zhuang ◽  
Liang Zhao ◽  
Liang-Yun Zhao ◽  
Ji-Quan Zhao ◽  
...  

2003 ◽  
Vol 49 (6) ◽  
pp. 433-438 ◽  
Author(s):  
H. FUSE ◽  
R. NISHIO ◽  
K. MURAKAMI ◽  
A. OKUMURA

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